Physio-Control, Inc.: 16 recalls on record

Recalls filed with 1 agency: FDA (16).

First recall on record: April 17, 2013. Most recent: May 13, 2026.

Risk classification: Class I: 3 · Class II: 12 · Class III: 1

Most recent recalls

DateAgencyProduct
May 13, 2026FDALIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99…Z-2065-2026
November 6, 2024FDALIFEPAK 15 (LP15) Model/Catalog Numbers: o 97577-000101 o 99577-000046 o 99577-000055 …Z-0230-2025
October 30, 2024FDASTERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP20 STERILIZABLE INTERNAL DEFIBRILLATI…Z-0142-2025
November 22, 2023FDALIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022Z-0303-2024
March 16, 2022FDAHeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-PakZ-0745-2022
April 8, 2020FDALifePAK 500 Automated External Defibrillator, model numbers: 3005400-XXX, U3005400-XXX, 3…Z-1633-2020
January 22, 2020FDALIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade…Z-0816-2020
March 6, 2019FDALIFEPAK 15 Monitor/Defibrillator Product Usage: The LIFEPAK(R) 15 Monitor/defibrillat…Z-0862-2019
December 20, 2017FDALIFEPAK(R) Electrode Starter Kits, Catalog # 11101-000017, MIN #3202784-009 The defib…Z-0187-2018
March 15, 2017FDAThe LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a p…Z-1257-2017
February 15, 2017FDALIFEPAK 12 Defibrillator/Monitor with End-Tidal CO2 option. The device is used in var…Z-1143-2017
February 15, 2017FDALIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option. Intended for use by tr…Z-1144-2017
June 22, 2016FDALIFEPAK15 monitor/defibrillator with End-Tidal C02 (EtC02) feature installed. Part n…Z-1993-2016
June 4, 2014FDALIFEPAK 1000 defibrillator. Affected Part Numbers: 320371500XXX The LP1000 (in AED mo…Z-1660-2014
July 31, 2013FDAThe LIFEPAK 500 Automated External Defibrillator is a semi-automatic defibrillator that u…Z-1773-2013
April 17, 2013FDAThe LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's numbers: 3200731-…Z-1082-2013

Questions about this company

How many recalls does Physio-Control, Inc. have?
Recalert has 16 U.S. recalls on record for Physio-Control, Inc., published between April 17, 2013 and May 13, 2026.
What was the most recent Physio-Control, Inc. recall?
FDA recall Z-2065-2026, published May 13, 2026: LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 99577-001957, 99577-001935, 99577-001964, 99577-001955, 99577-001956, 99577-001588, …
Which agencies have handled Physio-Control, Inc. recalls?
Physio-Control, Inc. appears as the recalling firm in recalls from: FDA (16).

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